Datex-Ohmeda recalls Aisys CS2 anesthesia machines due to risk of patient injury from incorrect circuit connections. All units with Auxiliary Common Gas Outlet (ACGO) option are affected. No specific remedy stated in recall.
Potential issue that may arise if the limb of a patient breathing circuit is mistakenly connected to the Auxiliary Common Gas Outlet (ACGO) port.
Datex-Ohmeda is recalling all Aisys CS2 anesthesia machines that have the Auxiliary Common Gas Outlet (ACGO) option. This could cause serious injury if a patient's breathing circuit is mistakenly connected to the ACGO port during use.
If a patient's breathing circuit is accidentally connected to the Auxiliary Common Gas Outlet (ACGO) port instead of the correct port, it could cause improper gas delivery. This might lead to inadequate anesthesia or oxygen supply, potentially causing serious injury or harm to the patient.
Medical professionals using the Aisys CS2 anesthesia machines with the ACGO option are affected. Patients receiving anesthesia through these machines are at risk if the circuit connection is incorrect.
Check if your Aisys CS2 machine has the ACGO option. All units with this configuration are affected. The product is sold with a GTIN of 00840682102292 and model number 1011-9050-000.
Verify if your Aisys CS2 machine has the Auxiliary Common Gas Outlet (ACGO) option installed.
The recall record does not state any remedy or action steps.
All Aisys CS2 machines with the Auxiliary Common Gas Outlet (ACGO) option are affected.
Check if your Aisys CS2 has the ACGO option. All units with this configuration are affected.
We’ve drafted a message you can send Datex-Ohmed: Aisys to request your refund or repair — edit it as you like.
Subject: Recall Z-0082-2025 — Datex-Ohmed: Aisys Datex-Ohmed: Aisys Hello, I own a Datex-Ohmed: Aisys that is covered by recall Z-0082-2025 from Datex-Ohmed: Aisys. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
